DermaRite Industries, LLC 2025-11-26 Health serious FDA
Health · FDA · Recall #FDA-D-0168-2026
KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge,… Recall
Issued November 26, 2025 · DermaRite Industries, LLC
In November 2025, DermaRite Industries, LLC recalled the KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
What you should do
- 1 Stop using KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact DermaRite Industries, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- DermaRite Industries, LLC
- Category
- Health
- Recall date
- November 26, 2025
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0168-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- DermaRite Industries, LLC has 11 recalls in our database, including 3 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.